Senior Clinical Research Associate
hace 1 semana
We are seeking a highly skilled Senior Clinical Research Associate to join our team at AbbVie.
The successful candidate will be responsible for ensuring successful protocol level execution of clinical study deliverables involving start-up, execution, and close-out.
Key Responsibilities:
- Ensure successful site-related study execution, including monitoring visits, site evaluations, site selection, and activation.
- Maintain clinical trial management systems containing all site-specific information and provide local regulatory and legal requirement expertise.
- Ensure adherence to federal regulations, Good Clinical Practices (GCPs), ICH Guidelines, and AbbVie Standard Operating Procedures (SOPs).
- Prepare and follow up site audits/inspections and provide input into the CAPA preparation.
- Responsible for coaching and mentoring CRAs and providing input into their development.
- Bachelor's degree or equivalent in a health-related field.
- Minimum 5 years of site monitoring experience.
- Strong analytical and critical thinking skills to evaluate complex issues.
- Excellent interpersonal skills with the ability to communicate persuasively.
- Demonstrated business ethics and integrity.
About AbbVie
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion.
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